Evidence map›Paper›PMID 21632941›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2011

NMDA receptor activation suppresses microtubule growth and spine entry.

Lukas C Kapitein, Kah Wai Yau, Susana Montenegro Gouveia, Wouter A van der Zwan, Phebe S Wulf, Nanda Keijzer, Jeroen Demmers, Jacek Jaworski, Anna Akhmanova, Casper C Hoogenraad

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
3.7field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

66 citing papers in PubMed, 112 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Functional Inhibition of Katanin Affects Synaptic Plasticity.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  7. Article
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  9. Differential regulation of MAP2 by phosphorylation events in proline-rich versus C-terminal domains.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2023
    Article
  10. Article
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  13. Review
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  15. More than a marker: potential pathogenic functions of MAP2.Frontiers in molecular neuroscience · 2022
    Article
  16. Article
  17. The synaptic life of microtubules.Current opinion in neurobiology · 2021
    Review
  18. Article
  19. Review
  20. Article

6 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 3 countries.

Lukas C KapiteinCell Biology, Faculty of Science, Utrecht University, 3584CH Utrecht, The Netherlands.
Kah Wai Yau
Susana Montenegro Gouveia
Wouter A van der Zwan
Phebe S Wulf
Nanda Keijzer
Jeroen Demmers
Jacek Jaworski
Anna Akhmanova
Casper C Hoogenraad
Society for Neuroscience · USUtrecht University · NLErasmus MC · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dynamic microtubules are important to maintain neuronal morphology and function, but whether neuronal activity affects the organization of dynamic microtubules is unknown. Here, we show that a protocol to induce NMDA-dependent long-term depression (LTD) rapidly attenuates microtubule dynamics in primary rat hippocampal neurons, removing the microtubule-binding protein EB3 from the growing microtubule plus-ends in dendrites. This effect requires the entry of calcium and is mediated by activation of NR2B-containing NMDA-type glutamate receptor. The rapid NMDA effect is followed by a second, more prolonged response, during which EB3 accumulates along MAP2-positive microtubule bundles in the dendritic shaft. MAP2 is both required and sufficient for this activity-dependent redistribution of EB3. Importantly, NMDA receptor activation suppresses microtubule entry in dendritic spines, whereas overexpression of EB3-GFP prevents NMDA-induced spine shrinkage. These results suggest that short-lasting and long-lasting changes in dendritic microtubule dynamics are important determinants for NMDA-induced LTD.

Indexed as

AnimalsCalciumCell Culture TechniquesDendritic SpinesHippocampusLong-Term Synaptic DepressionMicrotubule-Associated ProteinsMicrotubulesNeuronsRatsReceptors, N-Methyl-D-AspartateCalciumMAP2 protein, ratMapre3 protein, ratMicrotubule-Associated ProteinsNR2B NMDA receptorReceptors, N-Methyl-D-Aspartate

Identifiers

PMID21632941
PMCPMC6622869
OpenAlexW2144167875

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.